Internal investigator Work, Jobs in Camden, Gtl (with Salaries)

CRC Associate
ICON Plc —North London
- Full-time
- Nursing
- Bachelor's degree
- Organisational skills
- Employee assistance programme
3d
Technical Threat Investigator, Threat Intel Engineering - UK
OpenAI —London
- Full-time
- Scripting
- In-person
- AI
- Relocation assistance
Assistant Hub Officer
HM Revenue and Customs —Stratford
- £31,471 a year
- Part-time
- Hybrid work
- Microsoft Word
- Presentation skills
- Travel
- Work from home
10d
Programme Manager
Imperial College London —South Kensington
- £46,614 - £56,345 a year
- Part-time
- Management
- Annual leave
12d
Digital Investigations Analyst
Protection Group International —London
- Hybrid work
- Bilingual
- Research
- Annual leave
Quick apply
Global Financial Crimes Investigator
Bank of America —Bromley
- Full-time
- Bachelor's degree
- No degree
3d
Clinical Research Associate - Midlands
MSD —London
- Full-time
- Writing skills
- Bachelor's degree
- Travel
Senior Digital Investigations Analyst
Protection Group International —London
- Hybrid work
- Team management
- Annual leave
Quick apply
11d
Regulatory Scientist
Orchard Therapeutics —London
- Full-time
- Hybrid work
- Writing skills
- Bachelor's degree
- Computer skills
Quick apply
Counter Fraud Investigator
The Granite Group —Sevenoaks
- £26,350 - £34,800 a year
- Full-time
- Hybrid work
- Continuous improvement
- Organisational skills
- Flexible schedule
Quick apply
Professional Services Consultant
LexisNexis Risk Solutions —London
- Full-time
- Customer service
- Communication skills
- Employee assistance programme
- Employee discount
Senior Fraud Intelligence Analyst
marshmallow —London
- Full-time
- Hybrid work
- Analysis skills
- AI
- Analytics
12d
Senior Product Manager, FinCrime
Monzo —London
- £105,000 - £135,000 a year
- Remote
- Product management
- AI
- Work from home
- Flexible schedule
Clinical Operations Specialist (Finance)
GlaxoSmithKline —London
- Full-time
- Hybrid work
- Bachelor's degree
- AI
- Communication skills
22h
DS DES (Digital Exploitation Services), Specialist Operations
City of London Police —London
- Weekend availability
- Writing skills
- Leadership
- Communication skills
Medical Affairs Advisor
GlaxoSmithKline —London
- Full-time
- Databases
- Leadership
11d
Senior DFIR Investigator
Solis —London
- Full-time
- Hybrid work
- Presentation skills
- Mentoring
- Communication skills
Quick apply
Police Staff Investigator - Proactive Trident - 01
Metropolitan Police —Lewisham
- £37,510 - £40,519 a year
- Full-time
- English
- Presentation skills
- Communication skills
- Annual leave
12d
Vice President, International Medical Affairs
Viridian Therapeutics, Inc. —London
- £270,000 - £310,000 a year
- Full-time
- Management
- Doctoral degree
- Travel
Quick apply
Sr Clinical Development Scientist
Kite Pharma —London
- Full-time
- Doctoral degree
- Analysis skills
- Bachelor's degree

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CRC Associate

ICON Plc -
North London

Apply Now

Job details

Full-time
3 days ago

Benefits

Company pension
Employee assistance programme

Qualifications

Nursing
Clinical research
Stakeholder collaboration
Patient appointment coordination
Filing
Bachelor's degree
Organisational skills
Multidisciplinary collaboration
Good Clinical Practice (GCP)
Communication skills
Good Clinical Practice (ICH-GCP) guidelines

Full job description

Clinical Research Coordinator- Associate- Office Based

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

This role is with Accellacare , part of ICON's clinical research network, where you’ll play a key role in transforming the clinical trial experience for patients and sponsors alike. Our global site network is designed with one goal in mind: to deliver better access, greater efficiency, and improved outcomes in clinical research.

As a CRC Associate at ICON, you will support clinical research activities to ensure high-quality data, protocol adherence, and patient safety.

What You Will Do:

You will contribute to clinical coordination activities, taking responsibility for your deliverables and working collaboratively.

Key responsibilities include:

Supporting the setup, coordination, and day-to-day conduct of clinical studies in accordance with protocols, ICH-GCP, and applicable regulations.
Assisting with patient screening, informed consent documentation, and enrolment activities under the supervision of site staff.
Ensuring accurate and timely completion of source documents and electronic case report forms (eCRFs).
Organising and maintaining study files, essential documents, and Trial Master File (TMF) content to support audit-readiness.
Coordinating study visits, scheduling patient appointments, and ensuring required assessments and procedures are completed as per protocol.
Collaborating with monitors, investigators, and internal teams to resolve data queries and support continuous quality improvement.

Your Profile:

You will bring relevant clinical coordination experience, along with the following qualifications and skills.

Required qualifications and experience:

Bachelor's degree in life sciences, nursing, pharmacy, or a related discipline, or equivalent experience in a clinical or healthcare setting.
Initial experience in clinical research or a similar regulated environment is preferred.
Basic understanding of clinical trial processes, GCP guidelines, and regulatory requirements, with a strong willingness to learn.
Strong organisational skills with the ability to manage multiple tasks, priorities, and deadlines with accuracy.
High level of attention to detail and commitment to data quality and patient safety.
Effective communication and interpersonal skills, with the ability to work collaboratively with site staff and cross-functional teams.

#LI-Accellacare

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request .

Are you a current ICON Employee?

Apply Now

Refine Your Search

internal investigator jobs in camden, gtl

CRC Associate

Technical Threat Investigator, Threat Intel Engineering - UK

Assistant Hub Officer

Programme Manager

Digital Investigations Analyst

Global Financial Crimes Investigator

Clinical Research Associate - Midlands

Senior Digital Investigations Analyst

Regulatory Scientist

Counter Fraud Investigator

Professional Services Consultant

Senior Fraud Intelligence Analyst

Senior Product Manager, FinCrime

Clinical Operations Specialist (Finance)

DS DES (Digital Exploitation Services), Specialist Operations

Medical Affairs Advisor

Senior DFIR Investigator

Police Staff Investigator - Proactive Trident - 01

Vice President, International Medical Affairs

Sr Clinical Development Scientist

I want to receive the latest job alerts for internal investigator in camden, gtl

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